The objective of the Rheumatology Research Training Program at Hospital for Special Surgery (HSS) is to prepare outstanding physician and PhD candidates for 1) leadership positions in academic rheumatology and 2) careers as independent basic and clinical research investigators who will make important contributions to advancing understanding of and treatments for rheumatic diseases. To achieve this goal, HSS has created a unique environment of scientific, clinical and educational excellence that is highly focused on the adult and pediatric rheumatic diseases;has recruited investigators of the highest caliber as mentors for rheumatology trainees;and has fashioned a structured, interdisciplinary program to take full advantage of the strengths of the scientific environment at the Tri-institutional Complex on York Avenue. The training program is designed to provide 1) formal coursework;2) a focused research project under the supervision of a research sponsor;and 3) opportunities for personal development as an investigator. These activities are available in either basic research or clinical research disciplines. The trainees who have been supported by the HSS Rheumatology Research Training Grant and completed training since the last competitive renewal in 2004 have had a remarkable level of success with regard to research productivity and career development. All four MD trainees currently hold faculty appointments and the two PhD trainees moved on to desired university or industry positions. Two of the three current trainees already have achieved very strong publication records. The recent trainees also demonstrate the success of the program in strengthening the clinical research component. This record of success in training future leaders and contributors to advances in rheumatology research will continue to grow during the next five year cycle of this Rheumatology Research Training Program.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32AR007517-30
Application #
8655785
Study Section
Arthritis and Musculoskeletal and Skin Diseases Special Grants Review Committee (AMS)
Program Officer
Mancini, Marie
Project Start
1985-07-01
Project End
2015-04-30
Budget Start
2014-05-01
Budget End
2015-04-30
Support Year
30
Fiscal Year
2014
Total Cost
$83,188
Indirect Cost
$13,935
Name
Hospital for Special Surgery
Department
Type
DUNS #
622146454
City
New York
State
NY
Country
United States
Zip Code
10021
Rozo, Cristina; Chinenov, Yurii; Maharaj, Reena Khianey et al. (2017) Targeting the RhoA-ROCK pathway to reverse T-cell dysfunction in SLE. Ann Rheum Dis 76:740-747
Mavragani, Clio P; Sagalovskiy, Irina; Guo, Qiu et al. (2016) Expression of Long Interspersed Nuclear Element 1 Retroelements and Induction of Type I Interferon in Patients With Systemic Autoimmune Disease. Arthritis Rheumatol 68:2686-2696
Lally, Lindsay; Mandl, Lisa A; Huang, Wei-Ti et al. (2015) Pregnancy Does Not Adversely Affect Postoperative Pain and Function in Women With Total Hip Arthroplasty. J Clin Rheumatol 21:323-5
Lally, Lindsay; Pernis, Alessandra; Narula, Navneet et al. (2015) Increased rho kinase activity in temporal artery biopsies from patients with giant cell arteritis. Rheumatology (Oxford) 54:554-8
Rogatsky, Inez; Chandrasekaran, Uma; Manni, Michela et al. (2014) Epigenetics and the IRFs: a complex interplay in the control of immunity and autoimmunity. Autoimmunity 47:242-55
Crow, Mary K (2014) Type I interferon in the pathogenesis of lupus. J Immunol 192:5459-68
Lally, Lindsay; Lebovics, Robert S; Huang, Wei-Ti et al. (2014) Effectiveness of rituximab for the otolaryngologic manifestations of granulomatosis with polyangiitis (Wegener's). Arthritis Care Res (Hoboken) 66:1403-9
Lally, Lindsay; Spiera, Robert F (2013) Biomarkers in ANCA-associated vasculitis. Curr Rheumatol Rep 15:363
Wang, Lu; Gordon, Rachael A; Huynh, Linda et al. (2010) Indirect inhibition of Toll-like receptor and type I interferon responses by ITAM-coupled receptors and integrins. Immunity 32:518-30
Tzeng, Te-Chen; Chyou, Susan; Tian, Sha et al. (2010) CD11c(hi) dendritic cells regulate the re-establishment of vascular quiescence and stabilization after immune stimulation of lymph nodes. J Immunol 184:4247-57

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